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  1. Article ; Online: Long-Term Outcomes of Kidney Transplant Recipients With Primary Idiopathic Focal Segmental Glomerulosclerosis.

    Staeck, O / Halleck, F / Budde, K / Khadzhynov, D

    Transplantation proceedings

    2017  Volume 49, Issue 10, Page(s) 2256–2259

    Abstract: Background: Few data exist on recurrence rates, treatment response, and long-term outcomes in kidney transplant recipients (KTR) with primary focal segmental glomerulosclerosis (FSGS).: Methods: This retrospective, observational study included 1218 ... ...

    Abstract Background: Few data exist on recurrence rates, treatment response, and long-term outcomes in kidney transplant recipients (KTR) with primary focal segmental glomerulosclerosis (FSGS).
    Methods: This retrospective, observational study included 1218 consecutive KTR during 2002 to 2016. All patients with primary idiopathic FSGS were identified through application of strict diagnostic criteria. Outcomes were followed over an average of 70.4 months.
    Results: We identified 48 KTR (3.9%) with primary FSGS. Seven-year death-censored graft survival rate was 81% (primary FSGS) versus 85% (control) (P = .297). Eighteen KTR had FSGS recurrence (predicted incidence, 50% after 7 years). Seven-year death-censored graft survival rate in KTR with FSGS recurrence was significantly worse than in FSGS KTR without recurrence (63% versus 96%, P = .010). In the case of FSGS recurrence, a multi-modal treatment approach was applied, including plasma exchange (PE) (100% of patients), intravenous cyclosporine (50%), rituximab (61%), and the "Multiple Target Treatment" (39%). The median number of PE sessions was 27. Proteinuria decreased significantly and persistently during the course of treatment. Complete remission of FSGS was observed in 7 patients (39%); another 7 patients (39%) had partial remission (PE dependence was observed in 4 patients [22%]). Four patients (22%) with FSGS recurrence had early graft loss (<6 months after transplant) despite all treatment efforts.
    Conclusions: In KTR with primary FSGS, a high proportion of recurrence occurred, and recurrence was associated with significantly worse death-censored graft survival rates. However, a multi-modal treatment approach led to improvement of proteinuria and full or partial remission in most patients. Importantly, overall death-censored graft survival rate in KTR with primary FSGS was comparable with that in the control group.
    MeSH term(s) Adult ; Combined Modality Therapy ; Cyclosporine/administration & dosage ; Female ; Glomerulosclerosis, Focal Segmental/complications ; Glomerulosclerosis, Focal Segmental/mortality ; Glomerulosclerosis, Focal Segmental/therapy ; Graft Survival ; Humans ; Immunologic Factors/administration & dosage ; Kidney Transplantation/methods ; Kidney Transplantation/mortality ; Male ; Middle Aged ; Plasma Exchange/methods ; Postoperative Period ; Proteinuria/etiology ; Proteinuria/therapy ; Recurrence ; Remission Induction ; Retrospective Studies ; Rituximab/administration & dosage ; Survival Rate ; Treatment Outcome
    Chemical Substances Immunologic Factors ; Rituximab (4F4X42SYQ6) ; Cyclosporine (83HN0GTJ6D)
    Language English
    Publishing date 2017-12
    Publishing country United States
    Document type Journal Article ; Observational Study
    ZDB-ID 82046-5
    ISSN 1873-2623 ; 0041-1345
    ISSN (online) 1873-2623
    ISSN 0041-1345
    DOI 10.1016/j.transproceed.2017.10.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Immunologic Long-term Outcomes of Living-Related Kidney Transplantations Depending on the Donor-Recipient Relationship.

    Khadzhynov, D / Halleck, F / Lehner, L / Schmidt, D / Schrezenmeier, E / Budde, K / Staeck, O

    Transplantation proceedings

    2017  Volume 49, Issue 10, Page(s) 2265–2268

    Abstract: Background: The aim of this study is to analyze the long-term immunologic outcomes of living-related kidney transplantations depending on the donor-recipient relationship.: Methods: This retrospective single-center study included adult kidney ... ...

    Abstract Background: The aim of this study is to analyze the long-term immunologic outcomes of living-related kidney transplantations depending on the donor-recipient relationship.
    Methods: This retrospective single-center study included adult kidney transplant recipients (KTR) transplanted between 2000 and 2014. Among 1117 KTRs, 178 patients (15.9%) received living-related donations. Those patients were further categorized according to the donor-recipient relationship: 65 transplantations between siblings, 39 father-to-child (F-t-C) and 74 mother-to-child (M-t-C) donations. Allograft biopsies were performed for clinically suspected rejections. Data analysis included patient and graft survival, biopsy proven rejections (T-cell mediated [TCMR] or antibody mediated) and development of de novo donor-specific antibody. Outcome data were assessed over a period of a maximum 14 years.
    Results: There was no significant difference between the groups (F-t-C, M-t-C, and siblings) with regard to HLA-mismatches, prior kidney transplantations, time on dialysis, and cold ischemia time. Among KTRs with related donors, the type of relationship had no significant influence on graft survival. F-t-C and M-t-C pairs showed comparable incidences of TCMR at 7 years post-transplantation, both significantly exceeding the rate in sibling-to-sibling pairs (26.2% and 26.8% vs 10%, respectively; P = .043). A multivariate Cox regression analysis adjusted for recipient age, donor age, and HLA (A, B, DR)-mismatches identified both M-t-C- and F-t-C-donations as important independent risk factors for TCMR (hazard ratio: 8.13; P < .001 and hazard ratio: 8.09; P = .001, respectively). There was no significant difference between the groups concerning the incidence of antibody-mediated rejection and de novo donor-specific antibody.
    Conclusion: Our results indicate that parent-to-child kidney donation is an independent risk factor for TCMR.
    MeSH term(s) Adult ; Antibodies/immunology ; Family ; Female ; Graft Rejection/epidemiology ; Graft Rejection/immunology ; Graft Survival/immunology ; Humans ; Incidence ; Kidney/immunology ; Kidney Transplantation/adverse effects ; Kidney Transplantation/methods ; Living Donors ; Male ; Middle Aged ; Multivariate Analysis ; Proportional Hazards Models ; Retrospective Studies ; Risk Factors ; T-Lymphocytes/immunology ; Transplantation, Homologous
    Chemical Substances Antibodies
    Language English
    Publishing date 2017-12
    Publishing country United States
    Document type Evaluation Studies ; Journal Article
    ZDB-ID 82046-5
    ISSN 1873-2623 ; 0041-1345
    ISSN (online) 1873-2623
    ISSN 0041-1345
    DOI 10.1016/j.transproceed.2017.11.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Prolonged Low-Dose Prophylaxis With Valganciclovir in Cytomegalovirus-Negative Recipients of Kidney Transplants From Cytomegalovirus-Positive Donors Allows Seroconversion and Prevents Cytomegalovirus Disease.

    Halleck, F / Khadzhynov, D / Schrezenmeier, E / Lehner, L / Budde, K / Staeck, O

    Transplantation proceedings

    2017  Volume 49, Issue 10, Page(s) 2280–2284

    Abstract: Background: Cytomegalovirus-negative recipients of kidneys from cytomegalovirus (CMV)-positive donors (D+/R-) are at high risk to develop severe clinical manifestations of CMV disease. Long-term data about incidence and timing of CMV seroconversion, CMV ...

    Abstract Background: Cytomegalovirus-negative recipients of kidneys from cytomegalovirus (CMV)-positive donors (D+/R-) are at high risk to develop severe clinical manifestations of CMV disease. Long-term data about incidence and timing of CMV seroconversion, CMV disease, and the influence of prolonged valganciclovir prophylaxis on the clinical course of CMV infection are missing.
    Methods: We conducted a retrospective long-term study of 89 consecutive CMV D+/R- kidney transplant recipients transplanted between 2003 and 2012. All recipients received valganciclovir prophylaxis after transplantation (median 187 [126-261] days) with a median dose of 213 (181-338) mg/d. Long-term outcome was assessed over a maximum of 10 years post-transplant.
    Results: During follow-up (median 62 months) 60 of 89 (67%) patients had CMV seroconversion, and 29 of 89 (33%) developed symptomatic CMV disease. In addition, in 38 of the 60 (63%), seroconversion occurred during prophylaxis (median 154 days post-transplant), and in 22 patients, after the end of prophylaxis (median 320 days after transplantation). Baseline characteristics of the 2 groups did not differ significantly. Seroconversion during prophylaxis vs seroconversion after the end of prophylaxis was associated with significantly lower incidence of CMV disease (34% vs 73%, P = .007), less severe CMV disease (16% vs 64%, P < .001), and fewer organ manifestations (26% vs 64%, P = .006). The risk of CMV disease was limited to the first 475 days after transplantation. Valganciclovir resistance occurred in just 1 case (1%).
    Conclusions: Prolonged prophylaxis with low-dose valganciclovir allowed CMV seroconversion during prophylaxis in a high proportion of D+/R- patients. Seroconversion occurred after a median of 154 days and was associated with significantly lower incidence of CMV disease, less severe CMV disease, and fewer CMV complications.
    MeSH term(s) Adult ; Antiviral Agents/administration & dosage ; Antiviral Agents/therapeutic use ; Cytomegalovirus/drug effects ; Cytomegalovirus Infections/prevention & control ; Cytomegalovirus Infections/transmission ; Cytomegalovirus Infections/virology ; Drug Administration Schedule ; Female ; Ganciclovir/administration & dosage ; Ganciclovir/analogs & derivatives ; Humans ; Incidence ; Kidney Transplantation/adverse effects ; Longitudinal Studies ; Male ; Middle Aged ; Postoperative Complications/prevention & control ; Postoperative Complications/virology ; Pre-Exposure Prophylaxis/methods ; Retrospective Studies ; Seroconversion/drug effects ; Time Factors ; Tissue Donors ; Transplants/immunology ; Transplants/virology
    Chemical Substances Antiviral Agents ; valganciclovir (GCU97FKN3R) ; Ganciclovir (P9G3CKZ4P5)
    Language English
    Publishing date 2017-12
    Publishing country United States
    Document type Evaluation Studies ; Journal Article
    ZDB-ID 82046-5
    ISSN 1873-2623 ; 0041-1345
    ISSN (online) 1873-2623
    ISSN 0041-1345
    DOI 10.1016/j.transproceed.2017.10.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Impact of Pre-existing Comorbidities on Long-term Outcomes in Kidney Transplant Recipients.

    Kleinsteuber, A / Halleck, F / Khadzhynov, D / Staeck, A / Lehner, L / Duerr, M / Glander, P / Schmidt, D / Budde, K / Staeck, O

    Transplantation proceedings

    2018  Volume 50, Issue 10, Page(s) 3232–3241

    Abstract: Background: Outcomes of patients with end-stage renal disease are mainly affected by their comorbidities. Detailed data evaluating the impact of pre-transplant comorbidities on long-term outcome after kidney transplantation are largely missing.: ... ...

    Abstract Background: Outcomes of patients with end-stage renal disease are mainly affected by their comorbidities. Detailed data evaluating the impact of pre-transplant comorbidities on long-term outcome after kidney transplantation are largely missing.
    Methods: In a long-term retrospective analysis, we investigated 839 deceased donor kidney transplant recipients (KTRs) who received transplants between 1999 and 2014. The prevalence and impact of the most relevant comorbidities were studied in detail.
    Results: At the time of transplantation, 25% of KTRs had coronary artery disease (CAD), 16% had diabetes mellitus (DM), 11% had peripheral arterial disease (PAD), 8% had chronic heart failure (CHF), and 7% had cerebrovascular disease (CVD). KTRs with pre-existing CAD, DM, PAD, and CHF showed a significantly inferior patient survival. Multivariate analysis adjusting for all relevant factors and comorbidities confirmed CAD as most hazardous independent risk factor for premature death (hazard ratio [HR] 1.70; P = .002). A multivariate analysis revealed CHF and PAD as independent risk factors for death censored graft loss (HR 2.20; P = .003 and HR 1.80; P = .013). Diabetes was independently and significantly associated with T-cell- (HR 1.46; P = .020) and antibody-mediated rejections (HR 2.27; P = .030).
    Conclusions: Detailed quantification of the impact of pre-transplant comorbidities may facilitate the evaluation of transplant candidates, guide post-transplant follow-up, and may help to further refine prediction algorithms and allocation systems.
    MeSH term(s) Adult ; Aged ; Comorbidity ; Diabetes Mellitus/epidemiology ; Female ; Graft Survival ; Heart Failure/epidemiology ; Humans ; Kidney Failure, Chronic ; Kidney Transplantation/adverse effects ; Kidney Transplantation/mortality ; Male ; Middle Aged ; Multivariate Analysis ; Peripheral Arterial Disease/epidemiology ; Prevalence ; Proportional Hazards Models ; Retrospective Studies ; Risk Factors ; Transplant Recipients
    Language English
    Publishing date 2018-09-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 82046-5
    ISSN 1873-2623 ; 0041-1345
    ISSN (online) 1873-2623
    ISSN 0041-1345
    DOI 10.1016/j.transproceed.2018.08.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Digitalisierung in der Transplantationsnachsorge

    Pisarski, P. / Schmid, A. / Schiffer, M. / Pape, L. / Budde, K. / Halleck, F. / Staeck, O.

    Nieren- und Hochdruckkrankheiten

    2018  Volume 47, Issue 5, Page(s) 265

    Language German
    Document type Article
    ZDB-ID 184315-1
    ISSN 0300-5224
    Database Current Contents Medicine

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  6. Article ; Online: Donor-Recipient Matching Based on Predicted Indirectly Recognizable HLA Epitopes Independently Predicts the Incidence of De Novo Donor-Specific HLA Antibodies Following Renal Transplantation.

    Lachmann, N / Niemann, M / Reinke, P / Budde, K / Schmidt, D / Halleck, F / Pruß, A / Schönemann, C / Spierings, E / Staeck, O

    American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

    2017  Volume 17, Issue 12, Page(s) 3076–3086

    Abstract: De novo donor-specific HLA antibodies (dnDSA) are recognized as a risk factor for premature allograft failure. Determinants of DSA specificity are generated via the indirect allorecognition pathway. Here, we present supportive data for the relevance of ... ...

    Abstract De novo donor-specific HLA antibodies (dnDSA) are recognized as a risk factor for premature allograft failure. Determinants of DSA specificity are generated via the indirect allorecognition pathway. Here, we present supportive data for the relevance of predicted indirectly recognizable HLA epitopes (PIRCHE) to predict dnDSA following kidney transplantation. A total of 2787 consecutive kidney transplants performed between 1995 and 2015 without preformed DSA have been analyzed. De novo DSA were detected by single antigen bead assay. HLA epitope mismatches were determined by the HLAMatchmaker and PIRCHE approach and correlated in uni- and multivariate analyses with 10-year allograft survival and incidence of dnDSA. The PIRCHE-II score moderately predicted allograft survival. However, the predictive value of elevated PIRCHE-II scores >9 for the incidence of dnDSA was statistically significant (p < 0.001). In a multivariate Cox regression analysis adjusted for antigen mismatch and HLAMatchmaker epitopes, the PIRCHE-II score could be identified as an independent risk factor for dnDSA. The PIRCHE-II score independently from the antigen mismatch and HLAMatchmaker epitopes could be revealed as being a strong predictor for dnDSA. PIRCHE may help to identify acceptable mismatches with decreased risk of dnDSA and thus improve long-term renal allograft survival.
    MeSH term(s) Antigens/immunology ; Epitopes/immunology ; Female ; Follow-Up Studies ; Germany/epidemiology ; Glomerular Filtration Rate ; Graft Rejection/epidemiology ; Graft Rejection/immunology ; Graft Survival/immunology ; HLA Antigens/immunology ; Histocompatibility Testing ; Humans ; Incidence ; Isoantibodies/blood ; Isoantibodies/immunology ; Kidney Failure, Chronic/surgery ; Kidney Function Tests ; Kidney Transplantation/methods ; Male ; Middle Aged ; Prognosis ; Risk Factors ; Tissue Donors ; Transplantation, Homologous
    Chemical Substances Antigens ; Epitopes ; HLA Antigens ; Isoantibodies
    Language English
    Publishing date 2017-07-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2060594-8
    ISSN 1600-6143 ; 1600-6135
    ISSN (online) 1600-6143
    ISSN 1600-6135
    DOI 10.1111/ajt.14393
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Incidence of Infectious Disease and Malignancies After Rituximab Therapy in Kidney Transplant Recipients: Results From a Cohort in Germany.

    Schrezenmeier, E / Budde, K / Staeck, O / Lehner, L / Duerr, M / Khadzhynov, D / Dörner, T / Halleck, F

    Transplantation proceedings

    2017  Volume 49, Issue 10, Page(s) 2269–2273

    Abstract: Background: Rituximab is frequently used in solid organ transplantation off-label, especially in patients with renal allografts. Few data are available on the safety aspects of solid organ transplant recipients receiving rituximab. There is a knowledge ... ...

    Abstract Background: Rituximab is frequently used in solid organ transplantation off-label, especially in patients with renal allografts. Few data are available on the safety aspects of solid organ transplant recipients receiving rituximab. There is a knowledge gap on long-term follow-up data, in particular on infectious complications.
    Patients and methods: A retrospective observational registry study (German Registry on Autoimmune Diseases) comprising a total of 681 patients was conducted. The data of 63 adult kidney transplant recipients who received rituximab between 2006 and 2013 were used in this analysis.
    Results: Median follow-up was 42 (1-109) months. At least 1 severe infection occurred in 57% of patients. The median time between the first rituximab infusion and the first infection was 4 (1-48) months. Of the overall 88 infections, 74 were severe bacterial infections, 5 were severe viral infections, 3 were severe fungal infections, 2 were combined severe bacterial and fungal infections, and 4 were combined severe viral, fungal and bacterial infections. Seven patients died during the observational period, 2 of them due to infectious complications. In the observational period, 1 case of squamous cell carcinoma but no other malignancies were observed.
    Conclusion: Consistent with previous data, a high incidence of infections was observed after rituximab treatment in kidney transplant recipients. Most infections occurred within 6 months after rituximab initiation. With more than 3 years of follow-up, we were able to document a low incidence of secondary malignancies after rituximab with only 1 case in our cohort.
    MeSH term(s) Adult ; Aged ; Female ; Germany/epidemiology ; Humans ; Immunologic Factors/adverse effects ; Incidence ; Infection/chemically induced ; Infection/epidemiology ; Kidney Transplantation/adverse effects ; Male ; Middle Aged ; Neoplasms/chemically induced ; Neoplasms/epidemiology ; Registries ; Retrospective Studies ; Rituximab/adverse effects
    Chemical Substances Immunologic Factors ; Rituximab (4F4X42SYQ6)
    Language English
    Publishing date 2017-12
    Publishing country United States
    Document type Journal Article ; Observational Study
    ZDB-ID 82046-5
    ISSN 1873-2623 ; 0041-1345
    ISSN (online) 1873-2623
    ISSN 0041-1345
    DOI 10.1016/j.transproceed.2017.09.042
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Influence of pretransplant class I and II non-donor-specific anti-HLA immunization on immunologic outcome and graft survival in kidney transplant recipients.

    Staeck, Anja / Khadzhynov, Dmytro / Kleinsteuber, Anna / Lehner, Lukas / Duerr, Michael / Budde, Klemens / Lachmann, Nils / Halleck, Fabian / Staeck, Oliver

    Transplant immunology

    2020  Volume 63, Page(s) 101333

    Abstract: Background: Anti-HLA immunization determined by Panel Reactive Antibody (PRA) is known to have a negative impact on patient and graft survival. The predictive value of peak PRA (pPRA) on immunologic outcome, however, and the individual effects of anti- ... ...

    Abstract Background: Anti-HLA immunization determined by Panel Reactive Antibody (PRA) is known to have a negative impact on patient and graft survival. The predictive value of peak PRA (pPRA) on immunologic outcome, however, and the individual effects of anti-HLA class I and II antibodies remain uncertain.
    Methods: The influence of HLA immunization on immunologic outcome parameters and graft survival was investigated in 1150 adult patients without pretransplant donor-specific antibodies (DSA) and in a subgroup of elderly kidney recipients aged ≥ 65 (n = 264). Anti-HLA immunization was defined as a pPRA > 0%. We investigated the influence of class I and II pPRA by dividing all kidney recipients into four pPRA groups (0%, 1-20%, 21-80%, >80%).
    Results: Patients with non-donor-specific pretransplant anti-HLA immunization were at a higher risk for developing de novo DSA (49.9% vs. 18.7% p < 0.001), antibody mediated rejections (ABMR) (15.7% vs. 5.1%; p < 0.001), had a poorer death censored graft survival (69.2% vs. 86.2%; p < 0.001) and a higher decline of the calculated GFR. In elderly patients anti-HLA immunization only had a significant influence on the development of DSA (40.5% vs. 27.4%; p = 0.004). A multivariate model adjusted for all relevant factors revealed only class I but not class II pretransplant HLA immunization as a significant independent risk factor for de novo DSA, ABMR and death censored graft loss (HR 2.76, p < 0.001, HR 4.16, p < 0.001 and HR 2.07, p < 0.001, respectively).
    Conclusion: Mainly non-donor-specific pretransplant HLA class I immunization is an independent risk factor for the development of de novo DSA, ABMR and graft loss.
    MeSH term(s) Adult ; Aged ; Blood Grouping and Crossmatching/methods ; Female ; Graft Rejection/diagnosis ; Graft Rejection/immunology ; Graft Rejection/mortality ; Graft Survival ; HLA Antigens/immunology ; Histocompatibility Antigens Class I/immunology ; Histocompatibility Antigens Class II/immunology ; Humans ; Isoantigens/immunology ; Kidney Transplantation ; Male ; Middle Aged ; Predictive Value of Tests ; Preoperative Period ; Prognosis ; Survival Analysis ; Tissue Donors ; Treatment Outcome
    Chemical Substances HLA Antigens ; Histocompatibility Antigens Class I ; Histocompatibility Antigens Class II ; Isoantigens
    Language English
    Publishing date 2020-09-10
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1160846-8
    ISSN 1878-5492 ; 0966-3274
    ISSN (online) 1878-5492
    ISSN 0966-3274
    DOI 10.1016/j.trim.2020.101333
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Immunsuppression und Ergebnisse in der Nierentransplantation.

    Paliege, A / Bamoulid, J / Bachmann, F / Staeck, O / Halleck, F / Khadzhynov, D / Brakemeier, S / Dürr, M / Budde, K

    Der Urologe. Ausg. A

    2015  Volume 54, Issue 10, Page(s) 1376–1384

    Abstract: Background: Current immunosuppressive protocols effectively prevent acute rejection of renal allografts. Extensive drug toxicity and the deleterious effects of long-term immunosuppression are associated with significant morbidity and mortality.: ... ...

    Title translation Immunosuppression and its use in kidney transplantation.
    Abstract Background: Current immunosuppressive protocols effectively prevent acute rejection of renal allografts. Extensive drug toxicity and the deleterious effects of long-term immunosuppression are associated with significant morbidity and mortality.
    Objectives: The purpose of this article is to provide an overview over modern immunosuppressants and their unwanted side effects and to discuss strategies for improved long-term transplant survival.
    Methods: Review of the current topic-related literature and discussion of our own experience.
    Results: The use of antibody induction together with an initial combination therapy of calcineurin inhibitors, mycophenolate and steroids is recommended and results in excellent early outcomes. Detrimental effects include an increased incidence of infections, malignomas, and cardiovascular diseases. Long-term transplant survival is impaired by extensive drug toxicity and the frequent development of donor specific antibodies. Reduction of overall cumulative exposure to immunosuppressants or the reduction of specific toxic drugs such as calcineurin inhibitors and steroids may improve long-term results. Alternative immunosuppressants like mTOR inhibitors and belatacept appear to be effective and safe but their long-term effects on patient and allograft survival needs to be established in clinical trials.
    Conclusions: Current immunosuppressants provide effective protection from renal allograft rejection. However, their use is complicated by serious side effects. In the future, development of novel immunosuppressants and optimization of minimization strategies may help to improve long-term success after kidney transplantation.
    MeSH term(s) Cardiovascular Diseases/chemically induced ; Cardiovascular Diseases/prevention & control ; Evidence-Based Medicine ; Graft Rejection/etiology ; Graft Rejection/prevention & control ; Humans ; Immune System Diseases/chemically induced ; Immune System Diseases/prevention & control ; Immunosuppressive Agents/administration & dosage ; Immunosuppressive Agents/adverse effects ; Kidney Transplantation/adverse effects ; Neoplasms/chemically induced ; Neoplasms/prevention & control ; Risk Factors
    Chemical Substances Immunosuppressive Agents
    Language German
    Publishing date 2015-10
    Publishing country Germany
    Document type English Abstract ; Journal Article ; Review
    ZDB-ID 204041-4
    ISSN 1433-0563 ; 0340-2592 ; 0375-4685
    ISSN (online) 1433-0563
    ISSN 0340-2592 ; 0375-4685
    DOI 10.1007/s00120-015-3909-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: A novel tool for the identification of correlations in medical data by faceted search.

    Schmidt, Danilo / Budde, Klemens / Sonntag, Daniel / Profitlich, Hans-Jürgen / Ihle, Matthias / Staeck, Oliver

    Computers in biology and medicine

    2017  Volume 85, Page(s) 98–105

    Abstract: This work focuses on the integration of multifaceted extensive data sets (e.g. laboratory values, vital data, medications) and partly unstructured medical data such as discharge letters, diagnostic reports, clinical notes etc. in a research database. Our ...

    Abstract This work focuses on the integration of multifaceted extensive data sets (e.g. laboratory values, vital data, medications) and partly unstructured medical data such as discharge letters, diagnostic reports, clinical notes etc. in a research database. Our main application is an integrated faceted search in nephrology based on information extraction results. We describe the details of the application of transplant medicine and the resulting technical architecture of the faceted search application.
    Language English
    Publishing date 2017-06-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 127557-4
    ISSN 1879-0534 ; 0010-4825
    ISSN (online) 1879-0534
    ISSN 0010-4825
    DOI 10.1016/j.compbiomed.2017.04.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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